Relation between Nitrogen Nutrition, Cytokinin Activity and Tuberization in Solanum tuberosum

In water-culture experiments with potato plants (Solanum tuberosum L. cv. Ostara), the influence of tuberization initiated by a 7-day period of nitrogen withdrawal (discont. N) on the cytokinin activity in shoots, roots and exudate was studied. Plants with a constant supply of nitrogen (cont. N) were used as control. — Whereas no tuberization could be observed with cont. N, discont. N led to tuberization already 2 days after nitrogen withdrawal and all plants had been induced after another 4 days. In the roots of plants with discont. N, there was a temporary increase in cytokinin activity, whereas the activity decreased steadily with cont. N. In the exudate, cytokinin activity was greatly reduced during nitrogen withdrawal, whereas this activity in the exudate increased steadily with cont. N. — In the shoot with cont. N cytokinin activity decreased steadily, but with discont. N, after an initial decrease, the activity increased steeply. This increase is mainly or exclusively caused by a shift between the water-soluble and butanol-soluble fractions of the cytokinins in favour of the latter. The shift in cytokinin activity of the shoot is assumed to be in causal connection with an increased photosynthetic activity after the onset of tuber growth as ‘sink’ for assimilates.     

Nitrogen Fixation and Nitrogen Assimilation in a Temperate Saline Ecosystem

As nitrogen is known to be a limiting factor for plant growth, we were interested in the relationship between soil microbial activity and the nitrogen assimilation of 5 different halophytes from 4 saline sites near the lake “Neusiedlersee”, Austria. The following were studied between May and October 1985: nitrogen fixation (¹⁵N₂ and acetylene reduction): N-mineralization; several soil characteristics and in vivo nitrate reductase activity of roots and shoots of these plants. NO^?₃, org. N- and carboxylate contents of both roots and shoots, as well as the effect of NO^?₃-fertilization on the amounts of these substances, were determined on plants growing in the field during a 3-day period in September 1985. Fertilization led to a decrease in acetylene reduction activity at most sites, and an increase in the nitrate reductase activity of the shoots of all plants. Overall, carboxylate and organic nitrogen contents of these halophytes did not change in response to fertilization. Only in the roots of Aster tripolium and Atriplex hastata was there a marked increase in the nitrate reductase activity in response to fertilization. Species growing at the same site, such as Plantago maritima and Lepidium crassifolium showed contrasting levels of assimilatory activity. Apparent low rates of ammonification and nitrification were detected in soils from the 4 sites. The results are discussed in relation to the nitrogen and carbon economies of the microorganisms and plants.     

Distribution of NO3− reduction between roots and shoots of peachtree seedlings as affected by NO3− uptake rate

The distribution of NO₃^? reduction between roots and shoots was studied in hydro-ponically-grown peach-tree seedlings (Prunus persica L.) during recovery from N starvation. Uptake, translocation and reduction of NO₃^?, together with transport through xylem and phloem of the newly reduced N were estimated, using ¹⁵N labellings, in intact plants supplied for 90 h with 0.5 mM NH₄⁺ and 0.5, 1.5 or 10 mM NO₃^?. Xylem transport of NO₃^? was further investigated by xylem sap analysis in a similar experiment. The roots were the main site of NO₃^? reduction at all 3 levels of NO₃^? nutrition. However, the contribution of the shoots to the whole plant NO₃^? reduction increased with increasing external NO₃^? availability. This contribution was estimated to be 20, 23 and 42% of the total assimilation at 0.5, 1.5 and 10 mM NO₃^?, respectively. Both ¹⁵N results and xylem sap analysis confirmed that this trend was due to an enhancement of NO₃^? translocation from roots to shoots. It is proposed that the lack of NO₃^? export to the shoots at low NO₃^? uptake rate resulted from a competition between NO₃^? reduction in the root epidermis/cortex and NO₃^? diffusion to the stele. On the other hand, net xylem transport of newly reduced N was very efficient since ca 70% of the amino acids synthesized in the roots were translocated to the shoots, regardless of the level of NO₃^? nutrition. This net xylem transport by far exceeded the net downward phloem transport of the reduced N assimilated in shoots. As a consequence, the reduced N resulting from NO₃^? assimilation, principally occurring in the roots, was mainly incorporated in the shoots.     

Interaction between atmospheric and pedospheric nitrogen nutrition in spruce (Picea abies L. Karst) seedlings

The effect of NO₂ fumigation on root N uptake and metabolism was investigated in 3-month-old spruce (Picea abics L. Karst) seedlings. In a first experiment, the contribution of NO₂ to the plant N budget was measured during a 48 h fumigation with 100mm³m^?3 NO₂. Plants were pre-treated with various nutrient solutions containing NO₂ and NH₄⁺, NO₃^? only or no nitrogen source for 1 week prior to the beginning of fumigation. Absence of NH₄⁺ in the solution for 6d led to an increased capacity for NO₃^? uptake, whereas the absence of both ions caused a decrease in the plant N concentration, with no change in NO₃^? uptake. In fumigated plants, NO₂ uptake accounted for 20–40% of NO₃^? uptake. Root NO₃^? uptake in plants supplied with NH₄⁺plus NO₃^? solutions was decreased by NO₂ fumigation, whereas it was not significantly altered in the other treatments. In a second experiment, spruce seedlings were grown on a solution containing both NO₂ and NH₄⁺ and were fumigated or not with 100mm³m^?3 NO₂ for 7 weeks. Fumigated plants accumulated less dry matter, especially in the roots. Fluxes of the two N species were estimated from their accumulations in shoots and roots, xylem exudate analysis and ¹⁵N labelling. Root NH₄⁺ uptake was approximately three times higher than NO₃^? uptake. Nitrogen dioxide uptake represented 10–15% of the total N budget of the plants. In control plants, N assimilation occurred mainly in the roots and organic nitrogen was the main form of N transported to the shoot. Phloem transport of organic nitrogen accounted for 17% of its xylem transport. In fumigated plants, neither NO₃^? nor NH₄⁺ accumulated in the shoot, showing that all the absorbed NO₂ was assimilated. Root NO₃^? reduction was reduced whereas organic nitrogen transport in the phloem increased by a factor of 3 in NO₂-fimugated as compared with control plants. The significance of the results for the regulation of whole-plant N utilization is discussed.     

Ammonium nutrition increases water absorption in rice seedlings (Oryza sativa L.) under water stress

Water stress is a primary limitation on plant growth. In previous studies, it has been found that ammonium enhances the tolerance of rice plants to water stress, but how water is related to nitrogen form and water stress remains unknown. To study the effects of nitrogen form (NH ₄ ⁺ , NO ₃ ^? , and a mixture of NH ₄ ⁺ and NO ₃ ^? ) on the growth and water absorption of rice (Oryza sativa L.) seedlings, a hydroponic experiment with water stress, simulated by the addition of polyethylene glycol (PEG, 10% w/v, MW 6000), was conducted in a greenhouse. The results showed that, compared with non-water stress, under water stress, the fresh weight of rice seedlings increased by 14% with NH ₄ ⁺ nutrition, whereas it had decreased by about 20% with either NO ₃ ^? or mixed nitrogen nutrition. No significant difference was found in the transpiration rate of excised shoots or in xylem exudation of excised roots in NH ₄ ⁺ supply between the two water situations, whereas xylem flow decreased by 57% and 24% under water stress in NO ₃ ^? and mixed nutrition, and root hydraulic conductivity decreased by 29% and 54% in plants in NH ₄ ⁺ and NO ₃ ^? nutrition conditions, respectively. Although water absorption ability decreased in both NH ₄ ⁺ and NO ₃ ^? nutrition, aquaporin activity was higher in NH ₄ ⁺ than in NO ₃ ^? nutrition, regardless of water stress. We conclude that NH ₄ ⁺ nutrition can improve water handling in rice seedlings and subsequently enhance their resistance to drought.     

Mixed-nitrogen nutrition-mediated enhancement of drought tolerance of rice seedlings associated with photosynthesis,hormone balance and carbohydrate partitioning

To investigate whether mixed-N (NO₃ ^??+?NH₄ ⁺) nutrition can enhance rice growth under water-deficit condition, a hydroponic experiment in which rice plants were supplied with different N forms (NO₃ ^?, NH₄ ⁺ and mixed-N) was conducted, and the intrinsic mechanisms involved in photosynthesis, root-shoot carbon partitioning, and hormone signalling were investigated. Water stress was found to decrease rice biomass, leaf area, chlorophyll and Rubisco contents. However, mixed-N nutrition substantially alleviated these inhibitions compared with NO₃ ^? nutrition alone. Mixed-N nutrition also maintained a higher electron transport rate, actual photochemical efficiency of PSII, and non-photochemical quenching, causing higher photosynthesis and photochemical efficiency. Water stress up-regulated leaf sucrose-phosphate synthase (SPS), but down-regulated acid invertase (InvA). However, leaf InvA and root sucrose synthase in the cleavage direction (SSc) in NO₃ ^? nutrition was higher than that in mixed-N nutrition. Water stress decreased indole acetic acid (IAA) content in leaves and cytokinins content in roots, but their contents in mixed-N nutrition were higher than those in NO₃ ^? nutrition. In mixed-N nutrition, the up-regulation of SPS and IAA in leaves and the reduction of sucrose metabolism (SSc and InvA) in roots jointly resulted in the accumulation of sucrose in leaves and the inhibition of its transportation to roots, finally reducing the root:shoot ratio (R/S). The reduced R/S provides more photosynthates for shoots and increases the utilisation efficiency, thereby strengthening the water-deficit tolerance of plants. We concluded that the strengthened water-deficit tolerance in mixed-N-supplied rice was closely associated with higher accumulation of dry matter mainly via improvement of photosynthesis and photochemical efficiency, hormone balance, and coupling with root-shoot carbon partitioning.     

Nitrate nutrition enhances zinc hyperaccumulation in Noccaea caerulescens (Prayon)

Nitrate fertilization has been shown to increase Zn hyperaccumulation by Noccaea caerulescens (Prayon) (formerly Thlaspi caerulescens). However, it is unknown whether this increased hyperaccumulation is a direct result of NO₃ ^? nutrition or due to changes in rhizosphere pH as a result of NO₃ ^? uptake. This paper investigated the mechanism of NO₃ ^?-enhanced Zn hyperaccumulation in N. caerulescens by assessing the response of Zn uptake to N form and solution pH. Plants were grown in nutrient solution with 300 μM Zn and supplied with either (NH₄)₂SO₄, NH₄NO₃ or Ca(NO₃)₂. The solutions were buffered at either pH 4.5 or 6.5. The Zn concentration and content were much higher in shoots of NO₃ ^?-fed plants than in NH₄ ⁺-fed plants at pH 4.5 and 6.5. The Zn concentration in the shoots was mainly enhanced by NO₃ ^?, whereas the Zn concentration in the roots was mainly enhanced by pH 6.5. Nitrate increased Zn uptake in the roots at pH 6.5 and increased apoplastic Zn at pH 4.5. Zinc and Ca co-increased and was found co-localized in leaf cells of NO₃ ^?-fed plants. We conclude that NO₃ ^? directly enhanced Zn uptake and translocation from roots to shoots in N. caerulescens.     

Nitrogen Acquisition from Atmospheric NH3 by Lolium perenne

Ammonia (NH₃) is the third most abundant N species in the atmosphere and, due to various natural and anthropogenic sources, can reach high concentrations in some areas. While some plants show effects of toxicity, others are capable of using this N-form and grow well without any utilization of soil-N. Acquisition of atmospheric NH₃ will affect the acid-base balance of the plants as absorption and dissolution causes an alkalinisation (production of OH^?) and assimilation of NH₃ results in an acidification (generation of H⁺). As there is only a limited capacity for biochemical disposal of excess H⁺ in shoots, pH regulation may involve H⁺/OH^? extrusion into the media via roots and transport of (in)organic ions between roots and above-ground parts of the plant. Our aim therefore was to assess NH₃ acquisition by Lolium perenne and to study the effects of gas phase NH₃ on growth, acid-base balance and mineral composition of the plants. The experiments therefore included application of a range of ¹⁴NH₃ to the shoots and of ¹⁵N as NO₃^?, NH₄⁺ or NH₄NO₃ to the roots, from which the amount of gas phase NH₃ acquisition could be quantified. Analysis of the mineral composition provided data for calculation of acid-base balance as well as for water use efficiencies of the plants. The results indicate that over the range of NH₃ supplied, plants from all treatments could utilize gas-phase NH₃ as demonstrated by increases in growth and in N and C use efficiencies. Plants receiving NO₃^? via their roots had a higher capacity to use gaseous NH₃ than those growing with NH₄⁺. NH₃ assimilation in shoots reduced both the acid load with NH₄⁺ nutrition and the alkaline load with NO₃^? supply to the roots. The results of the experiments are discussed in relation to possible acid-base regulation mechanisms of the whole plant.     

Nitrogen isotope composition of tomato (Lycopersicon esculentum Mill. cv. T-5) grown under ammonium or nitrate nutrition

Studies that quantify plant δ¹⁵N often assume that fractionation during nitrogen uptake and intra-plant variation in δ¹⁵N are minimal. We tested both assumptions by growing tomato (Lycopersicon esculetum Mill. cv. T-5) at NH₄⁺ or NO^?₃ concentrations typical of those found in the soil. Fractionation did not occur with uptake; whole-plant δ¹⁵N was not significantly different from source δ¹⁵ N for plants grown on either nitrogen form. No intra-plant variation in δ¹⁵N was observed for plants grown with NH⁺₄. In contrast. δ¹⁵N of leaves was as much as 5.8% greater than that of roots for plants grown with NO^?₃. The contrasting patterns of intra-plant variation are probably caused by different assimilation patterns. NH⁺₄ is assimilated immediately in the root, so organic nitrogen in the shoot and root is the product of a single assimilation event. NO^?₃ assimilation can occur in shoots and roots. Fractionation during assimilation caused the δ¹⁵N of NO^?₃ to become enriched relative to organic nitrogen; the δ¹⁵N of NO^?₃ was 11.1 and 12.9% greater than the δ¹⁵N of organic nitrogen in leaves and roots, respectively. Leaf δ¹⁵N may therefore be greater than that of roots because the NO^?₃ available for assimilation in leaves originates from a NO^?₃ pool that was previously exposed to nitrate assimilation in the root.     

Role of sugars in nitrate utilization by roots of dwarf bean

Nitrate uptake and in vivo, nitrate reductase activity (NRA) in roots of Phaseolus vulgaris, L. cv. Witte Krombek were measured in nitrogen-depleted plants of varying sugar status, Variation in sugar status was achieved at the start of nitrate nutrition by excision, ringing, darkness or administration of sugars to the root medium. The shape of the apparent induction pattern of nitrate uptake was not influenced by the sugar status of the absorbing tissue. When measured after 6 h of nitrate nutrition (0.1 mol m^?3), steady state nitrate uptake and root NRA were in the order intact>dark>ringed>excised. Exogenous sucrose restored NRA in excised roots to the level of intact plants. The nitrate uptake rate of excised roots, however, was not fully restored by sucrose (0.03–300 mol m^?3). When plants were decapitated after an 18 h NO₃^? pretreatment, the net uptake rate declined gradually to become negative after three hours. This decline was slowed down by exogenous fructose, whilst glucose rapidly (sometimes within 5 min) stimulated NG^?₃ uptake. Presumably due to a difference in NO₃^? due to a difference in NO₃^? uptake, the NRA of excised roots was also higher in the presence of glucose than in the presence of fructose after 6 h of nitrate nutrition. The sugar-stimulation of, oxygen consumption as well as the release of ¹⁴CO₂ from freshly absorbed (U-¹⁴C) sugar was the same for glucose and fructose. Therefore, we propose a glucose-specific effect on NO₃^? uptake that is due to the presence of glucose rather than to its utilization in root respiration. A differential glucose-fructose effect on nitrate reductase activity independent of the effect on NO₃^? uptake was not indicated. A constant level of NRA occurred in roots of NO₃^? induced plants. Removal of nutrient nitrate from these plants caused an exponential NRA decay with an approximate half-life of 12 h in intact plants and 5.5 h in excised roots. The latter value was also found in roots that were excised in the presence of nitrate, indicating that the sugar status primarily determines the apparent rate of nitrate reductase decay in excised roots.     

Absorption of nitrate and ammonium ions by Lolium perenne from flowing solution cultures at low root temperatures

Lolium perenne L. cv. 23 (perennial ryegrass) plants were grown in flowing solution culture and acclimatized over 49 d to low root temperature (5°C) prior to treatment at root temperatures of 3, 5, 7 and 9°C for 41 d with common air temperature of 20/15°C day/night and solution pH 5·0. The effects of root temperature on growth, uptake and assimilation of N were compared with N supplied as either NH₄ or NO3 at 10 mmol m^?3. At any given temperature, the relative growth rate (RGR) of roots exceeded that of shoots, thus the root fraction (Rf) increased with time. These effects were found in plants grown with the two N sources. Plants grown at 3 and 5°C had very high dry matter contents as reflected by the fresh weight: freeze-dried weight ratio. This ratio increased sharply, especially in roots at 7 and 9°C. Expressed on a fresh weight basis, there was no major effect of root temperature on the [N] of plants receiving NHJ but at any given temperature, the [N] in plants grown with NHJ was significantly greater than in those grown with NO₃. The specific absorption rate (SAR) of NH⁺₄ was greater at all temperatures than SAR-NO₃. In plants grown with NH⁺, 3–5% of the total N was recovered as NH⁺₄, whereas in those grown with NO^?₃ the unassimilated NO^?₃ rose sharply between 7 and 9°C to become 14 and 28% of the total N in shoots and roots, respectively. The greater assimilation of NH⁺₄ lead to concentrations of insoluble reduced N (= protein) which were 125 and 20% greater, in roots and shoots, respectively, than in NO^?₃-grown plants. Plants grown with NH⁺₄ had very much greater glutamine and asparagine concentrations in both roots and shoots, although other amino acids were more similar in Concentration to those in NO^?₃ grown plants. It is concluded that slow growth at low root temperature is not caused by restriction of the absorption or assimilation of either NH⁺₄ or NO^?₃. The additional residual N (protein) in NH⁺₄ grown plants may serve as a labile store of N which could support growth when external N supply becomes deficient.     

Nitrate accumulation and growth of Aster tripolium L. with a continuous and intermittent nitrogen supply*

Abstract The ‘tidal salt marsh’ ecotype of the halophyte Aster tripolium L. was grown in a nutrient solution with either a continuous or an intermittent NO₃^? supply with either Cl^? or SO₄^2? as the alternative anion. With increasing periods of NO₃^? supply per week the rate of the dry weight increment increased. When NO₃^? was supplied for longer than 48 h per week, the dry weight and the organic-N content in the shoots hardly increased, whereas the NO₃^? content in shoots and roots increased further. With alternated supply of a nutrient solution containing NO₃^? with one containing Cl^?, the internal NO₃^? content in the shoot was lower than in shoots grown in solutions in which NO₃^? alternated with SO₄^2?. It is concluded, that NO₃^? does not have a specific function in osmoregulation.     

Mode of action of chlorsulfuron in a sensitive wheat (Triticum aestivum) cultivar: primary and secondary effects on nitrogen assimilation

Chlorsulfuron (15 g a.i. ha^-1) inhibited growth of wheat (Triticurn aestivum L. cv. Rongotea) especially on high nitrate (NO₃) supply. Decreased growth at high NO^-₃ was associated with higher concentrations of reduced nitrogen (N) and NO^-₃ in the shoots. Seven days after spraying (DAS), shoot dry weight (dry wt) of sprayed plants was similar with NO^-₃ or branched chain amino acids as main N supply but 28 DAS, shoot dry wt was greater with the amino acid treatment. One DAS, chlorsulfuron caused substantial decreases in extension of the youngest leaf and acetolactate synthase activity and valine content of shoots of plants supplied with NO^-₃ or branched chain amino acids. Total amino acid content of shoots was greater in sprayed plants than in unsprayed plants 1 DAS. Acetolactate synthase activity of sprayed plants supplied low NO^-₃ returned to normal 14–21 DAS. For sprayed plants transferred from low to high NO^-₃ supply 7, 14 or 21 DAS, shoot dry wt 50 DAS increased with increased time of transfer to high NO^-₃ while shoot NO^-₃ content decreased. Shoot NO₃ content of sprayed plants transferred to high NO^-₃ supply 7 or 14 DAS was similar to that in unsprayed plants at applied NO^-₃ concentrations which inhibited growth. It is concluded that inhibition of acetolactate synthase is likely to be the primary mode of action of chlorsulfuron in this wheat cultivar; data are consistent with the proposal that subsequent NO^-₃ accumulation can also inhibit growth.     

Implications of N acquisition from atmospheric NH3 for acid-bAse and cation-anion balance of Lolium perenne

In the atmosphere, ammonia (NH₃) is the third most abundant N species which, due to various natural and anthropogenic sources, can locally reach high concentrations. The acquisition of atmospheric NH₃ by plant shoots will lead to two opposing effects on acid-base balance. Absorption and dissolution of NH₃ will cause an alkalinisation, while the assimilation of NH₃ results in an acidification. Different rates of these processes would lead to an acid-base imbalance with consequences for the ionic balance of the plant. As there is only a limited capacity for biochemical disposal of excess H⁺ in shoots, pH regulation may involve a pattern of (in)organic ion flow between shoots and roots followed by H⁺/OH^? extrusion into the media via roots. The acquisition of NH₃ as additional N source should lead to a reduction in the ratio of mol H⁺/OH^? gained per mol N assimilated. We have recently investigated the NH₃ acquisition by Lolium perenne L. cv. Centurion and studied the effects of gas phase NH₃ on growth, acid-base balance and water-use efficiency. The experiments, therefore, included the application of a range of ¹⁴NH₃ to the shoots and of ¹⁵N as NO₃^?, NH₄⁺ or NH₄NO₃ to the roots. After a summary of the main conclusions from those experiments, we discuss the implications of the use of atmospheric NH₃ for the mineral composition of the plants. Over the range of NH₃ supplied, plants from all treatments could utilize gas-phase NH₃. Plants receiving NO₃^? via their roots had a higher capacity to use gaseous NH₃ than those growing with NH₄⁺. NH₃ assimilation in shoots reduced both the acid load with NH₄⁺ nutrition and the alkaline load with NO₃^? supply to the roots. The most significant effect of fumigation on the ion balance was an increase in K⁺ within all treatments, and this effect was highest in the NH₄⁺-fed plants. The results of the experiments support predictions of a combination of neutralizing biochemical reactions as well as transport of organic anion salts between shoots and roots as possible acid-base regulation mechanisms of the whole plant.     

Elevated CO2 plus chronic warming reduce nitrogen uptake and levels or activities of nitrogen‐uptake and ‐assimilatory proteins in tomato roots

Atmospheric CO₂ enrichment is expected to often benefit plant growth, despite causing global warming and nitrogen (N) dilution in plants. Most plants primarily procure N as inorganic nitrate (NO₃^?) or ammonium (NH₄⁺), using membrane‐localized transport proteins in roots, which are key targets for improving N use. Although interactive effects of elevated CO₂, chronic warming and N form on N relations are expected, these have not been studied. In this study, tomato (Solanum lycopersicum) plants were grown at two levels of CO₂ (400 or 700 ppm) and two temperature regimes (30 or 37°C), with NO₃^? or NH₄⁺ as the N source. Elevated CO₂ plus chronic warming severely inhibited plant growth, regardless of N form, while individually they had smaller effects on growth. Although %N in roots was similar among all treatments, elevated CO₂ plus warming decreased (1) N‐uptake rate by roots, (2) total protein concentration in roots, indicating an inhibition of N assimilation and (3) shoot %N, indicating a potential inhibition of N translocation from roots to shoots. Under elevated CO₂ plus warming, reduced NO₃^?‐uptake rate per g root was correlated with a decrease in the concentration of NO₃^?‐uptake proteins per g root, reduced NH₄⁺ uptake was correlated with decreased activity of NH₄⁺‐uptake proteins and reduced N assimilation was correlated with decreased concentration of N‐assimilatory proteins. These results indicate that elevated CO₂ and chronic warming can act synergistically to decrease plant N uptake and assimilation; hence, future global warming may decrease both plant growth and food quality (%N).     

Correlation of continuous ryegrass regrowth with cytokinin induced by root nitrate absorption

This study investigated the separate and combined effects of nitrate (NO₃ ^?) and cytokinin additions on continuous ryegrass regrowth after defoliation and the underlying mechanisms. Our results showed that frequent defoliation reduced the biomass of newly grown leaves and roots, the root soluble carbohydrate contents, the root vitality (an indicator of root absorption capacity), and the leaf contents of NO₃ ^?, zeatin and zeatin riboside (Z + ZR), and isopentenyl adenine and isopentenyl adenosine (IP + IPA). NO₃ ^?addition to the roots or leaves increased the biomass of newly grown leaves as well as the leaf contents of NO₃ ^?, Z + ZR, and IP + IPA without increasing the root-to-shoot delivery of endogenous cytokinin. Interestingly, cytokinin directly added to the leaves also increased the biomass of newly grown leaves and their Z + ZR and IP + IPA contents, suggesting that nitrate-induced leaf cytokinin production mediates the growth-promoting effects of nitrate. We also found that cytokinin had a direct whereas NO₃ ^? had an indirect effect on the biomass of newly grown leaves. Taken together, our results indicate that leaf cytokinin production induced by NO₃ ^? absorbed through the roots plays a key role in continuous ryegrass regrowth after defoliation.     

Root growth as a function of ammonium and nitrate in the root zone

We examined the effect of soil NH₄⁺ and NO₃^? content upon the root systems of field-grown tomatoes, and the influence of constant, low concentrations of NH₄⁺ or NO₃^? upon root growth in solution culture. In two field experiments, few roots were present in soil zones with low extractable NH₄⁺ or NO₃^?; they increased to a maximum in zones having 2μg-N NO₃^? g^?1 soil and 6 μg-N NO₃⁼ g^?1 soil, but decreased in zones having higher NH₄⁺ or NO₃^? levels. Root branching was relatively insensitive to available mineral nitrogen. Plants maintained in solution culture at constant levels of NH₄⁺ or NO₃^?, had similar shoot biomass, but all root parameters – biomass, length, branching and area – were greater under NH4 nutrition than under NO₃^?. These results suggest that the size of root system depends on a functional equilibrium between roots and shoots (Brouwer 1967) and on the balance between soil NH₄⁺ and NO₃^?.     

Impact of Atmospheric Sulfur Deposition on Sulfur Metabolism in Plants: H2S as Sulfur Source for Sulfur Deprived Brassica oleracea L.

Brassica oleracea L. was rather insensitive to atmospheric H₂S: growth was only negatively affected at ≥0.4 μl I^?1. Shoots formed a sink for H₂S and the uptake rate showed saturation kinetics with respect to the atmospheric concentration. The H₂S uptake rate was high in comparison with other species, which may reflect the high sulfur need of Brassica. The net uptake of sulfate by roots of hydroponically grown plants was substantially reduced after one week of exposure to 0.25 μl l^?1 H₂S, indicating that plants switched in part from sulfate to H₂S as sulfur source for plant growth. Plants were sulfur deficient after two weeks of sulfur deprivation, illustrated by reduced growth, which was more pronounced for shoots than for roots, and in enhanced shoot dry matter content. The latter could for the greater part be attributed to enhanced levels of soluble sugars and starch. Sulfur deficiency was further characterized by a low pigment content, extremely low levels of sulfate and water-soluble non-protein thiols, and by enhanced levels of nitrate and free amino acids, particularly in the shoots. Furthermore, sulfur deficient plants contained a lower total lipid content in shoots, whereas its content in roots was unaffected. The level of sulfolipids was decreased in both roots and shoots. When sulfur deprived plants were exposed to 0.25 μl I^?1 H₂S for one week, all sulfur deficiency symptoms were abolished and growth was restored. Furthermore, plants were able to grow with 0.4 μl I^?1 H₂S as the sole sulfur source. Water-soluble non-protein thiol content was enhanced in both shoots and roots of H₂S exposed plants, irrespective of the sulfate supply to the roots, whereas plants grown with H₂S as sole sulfur source contained very low sulfate levels. The interaction between atmospheric and pedospheric sulfur nutrition in plants is discussed.     

Nitrate Absorption and Acetylene Reduction by Soybeans during Reproductive Development

Nodulated and unnodulated soybeans (Glycine max [L.] Merr.) were grown in N-free or N-containing nutrient solutions, respectively. Starting at the initial flowering stage, and throughout reproductive growth, the NO₃- absorption capacity of roots of intact plants from both treatments was determined in short-term uptake experiments. Acetylene reduction activity was determined for nodulated plants. Nitrate absorption rate, expressed on a root dry weight basis, was greatest at early flowering for both nodulated and unnodulated plants. At 33 days after germination, the NO₃^- absorption rate of unnodulated plants was twice as great as that of nodulated plants. During the remainder of the sampling period, NO₃^- absorption rates of both nodulated and unnodulated plants decreased progressively and similarly. Maximum nodule specific activity occurred 30 days after germination, or initial flowering. However, maximum total C₂H₂ reduction activity, oner plant basis, was observed during the early stages of pod-filling. Compared to unnodulated plants dependent on NO₃^- assimilation, nodulated plants were smaller, had less N in vegetative tissues, and produced less seed per plant. We suggest that the higher NO₃^- absorption rate of unnodulated soybean roots, particularly during early reproductive growth, may have reflected a more favorable supply of photosynthate translocated to the roots from larger, more vigorous, non-N-stressed shoots.     

Differential effects of mineral and organic N sources,and of ectomycorrhizal infection by Hebeloma cylindrosporum,on growth and N utilization in Pinus pinaster

The effect of ectomycorrhizal association of Pinus pinaster with Hebeloma cylindrosporum was investigated in relation to the nitrogen source supplied as mineral (NH₄⁺ or NO₃^?) or organic N (L ‐glutamate) and at 5 mol m^?3. Plants were grown for 14 and 16 weeks with mineral and organic N, respectively, and samples were collected during the last 6 weeks of culture. Total fungal biomass was estimated using glucosamine amount and its viability was assessed using the glucosamine to ergosterol ratio. Non‐mycorrhizal plants grew better with NH₄⁺ than with NO₃^? and grew very slowly when supplied with L ‐glutamate. The presence of the fungus decreased the growth of the host plant with mineral N whereas it increased it with L ‐glutamate. Whatever the N source, most of the living fungal biomass was associated with the roots, whereas the main part of the total biomass was assayed outside the root. The form of mineral N did not significantly affect N accumulation rates over the 42 d in control plants. In mycorrhizal plants grown on either N source, the fungal tissues developing outside of the root were always the main N sink. The ectomycorrhizal association did not change ¹⁵NH₄⁺ uptake rate by roots, suggesting that the growth decrease of the host‐plant was related to the carbon cost for fungal growth and N assimilation rather than to a direct effect on NH₄⁺ acquisition. In contrast, in NO₃^?‐grown plants, in addition to draining carbon for NO₃^? reduction the fungus competed with the root for NO₃^? uptake. With NH₄⁺ or NO₃^? feeding, although mycorrhizal association improved N accumulation in shoots, we concluded that it was unlikely that the fungus had supplied the plant with N. In L ‐glutamate‐grown plants, the presence of the fungus increased the proportion of glutamine in the xylem sap and improved both N nutrition and the growth rate of the host plant.